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FDA Approves Seno Medical's Ground-Breaking Breast Cancer Diagnostic Technology

FDA Approves Seno Medical s Ground-Breaking Breast Cancer Diagnostic Technology
Seno s Imagio Breast Imaging System helps physicians differentiate between benign and malignant breast lesions using a novel combination of ultrasound and opto-acoustic technology.
San Antonio, TX, Jan. 19, 2021 (GLOBE NEWSWIRE) The Center for Devices and Radiological Health (CDRH) of the US Food & Drug Administration (FDA) has granted Texas-based
Seno Medical Instruments, Inc. (Seno)
premarket approval (PMA) for its groundbreaking
diagnostic breast cancer imaging technology that helps physicians better differentiate between benign and malignant breast lesions. The company s Imagio
Breast Imaging System uses non-invasive opto-acoustic ultrasound (OA/US) technology to provide information on suspicious breast lesions in real time, helping providers characterize and differentiate masses that may - or may not - require more invasive diagnostic evaluation. ....

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Investegate |Seno Medical Announcements | Seno Medical: FDA Approves Seno Medical's Ground-Breaking Breast Cancer Diagnostic Technology

FDA Approves Seno Medical’s Ground-Breaking Breast Cancer Diagnostic Technology
Seno’s Imagio® Breast Imaging System helps physicians differentiate between benign and malignant breast lesions using a novel combination of ultrasound and opto-acoustic technology.
San Antonio, TX, Jan. 19, 2021 (GLOBE NEWSWIRE) The Center for Devices and Radiological Health (CDRH) of the US Food & Drug Administration (FDA) has granted Texas-based
Seno Medical Instruments, Inc. (Seno)
premarket approval (PMA) for its groundbreaking
diagnostic breast cancer imaging technology that helps physicians better differentiate between benign and malignant breast lesions. The company’s Imagio
® Breast Imaging System uses non-invasive opto-acoustic ultrasound (OA/US) technology to provide information on suspicious breast lesions in real time, helping providers characterize and differentiate masses that may - or may not - require more invasive diagnostic evaluation. ....

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